On-Site CQV Project Lead - GMP Viral Vector Facility
Verista, Inc.
Verista, Inc. is seeking a Project Manager SME to lead the C&Q delivery team for a GMP viral vector facility build-out in Devens, MA. The role requires integrating staffing, schedule logic, earned-value tracking, and change control to ensure qualification and commissioning readiness. You will coordinate resources for SAT/IOQ/PQ windows, drive risk management, and report progress through green/blue tag milestones, with anticipated extension through April 2027. On-site, full-time, in Devens. #J-18808-Ljbffr Verista, Inc.
- Verista is seeking a Project Manager SME to lead the C&Q delivery team for a GMP viral vector facility build-out in Devens, MA. You will manage staffing, scheduling, and governance... .... The role requires 8-12+ years in GMP CQV leadership, proven capital project delivery, and...WebsiteFacilities
- ...MA is seeking a Senior CQV Engineer to lead C&Q deliverables for facilities, utilities, HVAC, cleanrooms... ...activities. This on-site role requires field-capable... ...has 8-12+ years of GMP CQV experience in biologics... ...and the ability to drive projects to #J-18808-Ljbffr...WebsiteFacilities
- Verista is seeking a Senior CQV Engineer to lead C&Q deliverables for facilities, utilities, HVAC,... ...interfaces in a Devens, MA site. You will drive design review... ...compliance and timely project closeout. This on-site, full... ...years CQV experience in GMP environments and strong communication...WebsiteFacilitiesFull time
- Verista, Inc. is seeking a Lead CQV SME / Lead Validation Engineer to provide senior... ...C&Q lifecycle for a wide range of facilities, utilities, equipment, and instruments. This role is on-site in Devens, MA and requires 15+ years of GMP CQV experience and strong regulatory...WebsiteFacilities
$107.8k - $168.01k
Job Overview We are seeking a Project Manager SME to lead the C&Q delivery team for a GMP viral vector facility build-out in Devens, MA,... ...equivalent required 8-12+ years GMP CQV project leadership CQV... ...requires the ability to be on-site, full-time in Devens, MA. Benefits...WebsiteFacilitiesFull timeTemporary work$87.78k - $161.65k
Lead CQV SME / Lead Validation Engineer We are... ...mixed portfolio of facility, utility, process equipment... ...best practices, project objectives, and... ...Acceptance Testing (FAT), Site Acceptance Testing... .... 15+ years in GMP CQV, ideally across biologics, viral vector, cell therapy, gene...WebsiteFacilitiesFull timeTemporary work$107.8k - $168.01k
...Overview: We are seeking a Project Manager SME to lead the C&Q delivery team for a GMP viral vector facility build-out in Devens, MA, covering... ...: Own day-to-day CQV delivery Interface with owner... ...facility startup ~ Strong owner/site stakeholder management ~...WebsiteFacilitiesFull timeTemporary workWork experience placement- ...Myers Squibb is seeking a Senior Manager for GMP Maintenance to lead the 24/7 maintenance team supporting the Devens Site Biologics Manufacturing Operations. This role... ...involves ensuring operational readiness of GMP facilities and developing maintenance strategies to...WebsiteFacilities
- Verista, Inc. in Devens, MA is seeking a Senior CQV Engineer to lead commissioning and qualification for facilities, utilities, HVAC, and cleanrooms within GMP manufacturing. You will coordinate PSSR, TOP reviews, and turnover evidence while guiding cross‑functional teams...Facilities
$80.47k - $123.51k
...are seeking a Senior CQV Engineer to lead C&Q deliverables and field coordination for facilities, utilities, HVAC, cleanrooms... .../utilities CQV in GMP manufacturing,... ...pharmaceutical capital projects Hands‑on HVAC/cleanroom... ...the ability to be on‑site, full‑time in Devens,...WebsiteFacilitiesFull timeTemporary workWork experience placement$120.37k - $145.86k
...Summary The Senior Manager, GMP Maintenance leads the 24/7 GMP Maintenance team that supports Devens Site Biologics Manufacturing Operations... ...that GMP manufacturing facilities, systems, and equipment are... ...effectively to cross‑functional project teams. Working knowledge of...WebsiteFacilitiesHourly payFull timeTemporary workSummer workLocal area- ...Gmp Assistant Manager The Gmp Assistant Manager is responsible... ...Manager works closely with site leadership to ensure staffing... ...to Gmp cleaning personnel and lead staff. Coordinate shift activities... ...experience within janitorial, facilities services, Gmp, pharmaceutical,...WebsiteFacilitiesWork at officeLocal areaAll shiftsFlexible hoursShift workAfternoon shift
- ...Validation Engineer to plan, schedule, and track validation projects across GMP facilities and equipment. You will develop detailed protocols and... ...including SIP validation. You will generate documentation, lead validation reports, and support customers with technical insight...WebsiteFacilities
- A leading company in the pharmaceutical sector is seeking a Contractor Field QA Specialist at their Single Use Facility in Devens, MA. This role is responsible for ensuring quality compliance and oversees QA activities on-site. The ideal candidate will have a strong background...WebsiteFacilitiesFor contractorsNight shift
$70.49k - $113.52k
Job Overview We are seeking a Senior CQV Engineer to lead C&Q documentation, vendor leveraging, walkdowns... ..., and qualification execution for viral vector drug substance process equipment and... ...validation SME Location & Schedule On‑site, full‑time in Devens, MA. Salary...WebsiteFull timeTemporary work$87.78k - $145.31k
Verista is seeking a Lead Validation Engineer to oversee CQV execution activities in Harvard, MA. The successful candidate will have over... ...and will lead teams to ensure compliance with GMP standards. This full-time on-site role offers a salary range of $87,780 to $145,30...WebsiteFull time- Bristol Myers Squibb EU Policy is seeking a Senior Manager, GMP Maintenance to lead the 24/7 team supporting Biologics Manufacturing... .... The role involves ensuring operational readiness of GMP facilities and developing maintenance strategies to maximize performance...Facilities
$101.01k - $122.4k
...otherwise, this role is "On‑Site" at the location... ...electrical elements of new projects including development... ...vendors and Third Party Facilities Management company.... ...site management and/or lead, working independently... ...facilities, as well as GMP experience. Effective...WebsiteFacilitiesFull timeTemporary workFor contractors- ...intermediates and manufactured products, and other GMP processes as required. Performs review and... ...audit readiness of the manufacturing facility and support areas. 4. Supports return to... ...is in compliance with corporate and site procedures, cGMP regulations, and other industry...WebsiteFacilitiesShift workWeekend work
$110.2k - $151k
...Manager - Construction & Facilities About Us Founded in 201... ...diverse perspectives lead to better outcomes. Job... ..., MEP services, and site and civil work. Reporting... ...ensure on‑time, on‑budget project delivery. Key... ...structures (AIA, NEC, lump sum, GMP), MEP systems, and...WebsiteFacilitiesContract workFor contractorsFor subcontractorLocal area- ...organization at the Single Use Facility (SUF) in Devens, MA. The... ...productivity within the group or project. • Builds relationships internally... ...to also have knowledge of GMP Manufacturing operations and processes... ...improvement and enhance site quality system efficiencies. •...WebsiteFacilitiesFor contractorsWork experience placementMonday to Thursday
- ...and JMP for data analysis Familiarity with GMP documentation and electronic data systems.... ...role is based at Devens Cell Therapy Facility (CTF). This role is responsible for assessing... ...deviation prevention and closure through site quality systems. Collaborate with cross-functional...WebsiteFacilitiesWork at office
- ...standardized solutions at any of their facilities regardless of physical... ...resources available at that site. We are seeking a Support System... ...manufacturing operations in a GMP-regulated environment. You... ...Manage continuous improvement projects. Be an ambassador who embodies...WebsiteFacilitiesLocal area
$70.49k - $118.06k
...complete documentation in compliance with GMP/GDP standards Work collaboratively with engineering... ...Engineering preferred) 3-8 years of CQV/validation experience Hands‑on experience... ...This role requires the ability to be on‑site, full‑time in Devens, MA. National (US)...WebsiteFull timeTemporary work$146.4k - $204.93k
...world's most exciting projects in a dynamic environment... ...Commissioning and Qualification Lead - Pharmaceutical / Life... ...will support complex GMP capital projects, with... ...workstreams supporting facilities, utilities, process... ..., vendors, and site operations. Support project...WebsiteFacilitiesFull timeTemporary workFor contractorsLocal area- ...Role Description This is a full-time, on-site Warehouse Driver role based in Littleton, MA. The Warehouse Driver is responsible for... ...and unloading products to and from customer locations and branch facilities. Day-to-day tasks include assisting with shipping and receiving...WebsiteFacilitiesFull time
- Peak Technologies is seeking a Senior Solutions Engineer to lead and manage complex projects across Littleton, MA and Eagan, MN, collaborating with the sales team to craft technology strategies and solutions. The role evolves toward specialist and post-sales focus, delivering...Website
$89.53k - $108.49k
...role maintains quality oversight, ensures GMP compliance, and supports real‑time quality... ...concerns. Train new team members on routine facility Quality tasks. Support return‑to‑service... ...QA review complies with corporate and site procedures, cGMP regulations, and industry...WebsiteFacilitiesFull timeMonday to FridayShift workAfternoon shift- ...to supervise craft workers at the Bristol-Myers Squibb Biologics Facility in Harvard, MA. This role involves ensuring safety compliance... ...efficiency. The position requires physical endurance to meet job demands and manage site conditions. #J-18808-Ljbffr The Brock Group IncWebsiteFacilities
- ...quality oversight and ensuring GMP compliance in day‑to‑day... ...Available: Monday - Friday, On‑site Afternoon Shift (2 p.m. - 10:3... ...Provide training on routine facility quality tasks for new team members... ...coordinate with higher‑level leads or supervisors, and apply appropriate...WebsiteFacilitiesMonday to FridayShift workAfternoon shift
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